In the journey to support women affected by Lichen Sclerosus Vulvae, the Nixarian Foundation stands as a beacon of hope and action. This blog highlights the importance of the fundamental pillars that support the foundation: disseminating, educating and researching about lichen sclerosus. Three actions that seek to illuminate the path towards understanding, well-being and the search for innovative and effective solutions.
Disseminate: accessible knowledge
Disseminate accurate information about
Lichen Sclerosus Vulvae
is essential to break down barriers of stigma and ignorance. The Nixarian Foundation is leading this effort, shining a light on the reality of those facing this condition and building bridges to empathy and community support.
How do we do it?
Through
conferences
in which professionals in the sector are made aware of the importance of this disease and with the Book
I have Vulvar Lichen Sclerosus What do I do now?
. It seeks to raise awareness about LEV and all proceeds are donated to the Foundation.
Training: creating experts
Training health professionals is vital for all women to be diagnosed effectively and early, in order to give them the appropriate treatment and recover their quality of life.
How do we do it?
We provide training through different
courses
both theoretical and practical, where the doctors will become experts in the
Liquenia treatment.
Vulvar lichen sclerosus research: the ongoing search for solutions
The Nixarian Foundation is committed to fostering research
research
by collaborating with experts and supporting projects that seek to discover new treatment approaches, improve quality of life and ultimately find the best solution for lichen sclerosus vulvae.
Outreach, education and research are intertwined to shape a future where lichen sclerosus vulvae does not limit women’s well-being and opportunities. Together, the Nixarian Foundation and the community create an echo of hope, progress and action.
